FDA 510(k) K160420, SpeqT, by Signostics Limited

510(K) Number: K160420
Device Name: SpeqT
Manufacturer: Signostics Limited
Device Classification Name: system, imaging, pulsed echo, ultrasonic
Regulation Number: 892.1560
Classification Product Code: IYO
Date Received: 02/16/2016
Decision Date: 03/21/2016
Regulation Medical Specialty: Radiology